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GCSH antibody

This Rabbit Polyclonal antibody specifically detects GCSH in WB and IF. It exhibits reactivity toward Human, Mouse and Rat.
Catalog No. ABIN7257311

Quick Overview for GCSH antibody (ABIN7257311)

Target

See all GCSH Antibodies
GCSH (Glycine Cleavage System H Protein (GCSH))

Reactivity

  • 39
  • 10
  • 10
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 37
  • 2
Rabbit

Clonality

  • 38
  • 1
Polyclonal

Conjugate

  • 13
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This GCSH antibody is un-conjugated

Application

  • 31
  • 15
  • 13
  • 13
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB), Immunofluorescence (IF)
  • Characteristics

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogen

    Recombinant fusion protein of human GCSH (NP_004474.2).

    Isotype

    IgG
  • Application Notes

    WB 1:500-1:2000 IF 1:50-1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    GCSH (Glycine Cleavage System H Protein (GCSH))

    Alternative Name

    GCSH

    Background

    Degradation of glycine is brought about by the glycine cleavage system, which is composed of four mitochondrial protein components: P protein (a pyridoxal phosphate-dependent glycine decarboxylase), H protein (a lipoic acid-containing protein), T protein (a tetrahydrofolate-requiring enzyme), and L protein (a lipoamide dehydrogenase). The protein encoded by this gene is the H protein, which transfers the methylamine group of glycine from the P protein to the T protein. Defects in this gene are a cause of nonketotic hyperglycinemia (NKH). Two transcript variants, one protein-coding and the other probably not protein-coding,have been found for this gene. Also, several transcribed and non-transcribed pseudogenes of this gene exist throughout the genome.

    Molecular Weight

    Observed_MW: 19 kDa

    Calculated_MW: 18 kDa

    Gene ID

    2653

    UniProt

    P23434
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